NOTE: There are no deadlines for IRB agendas. Submissions are placed on an agenda based on a combination of:
-date received,
-type of research / investigational product,
-risk,
-expertise needed for review,
-and space available on the agenda.
Generally, it is the goal of the IRB to assign submissions to agendas approximately 2 weeks to 30 days in advance of a meeting date.
If you wish to attend and observe an IRB meeting you must contact the IRB staff to schedule in advance of the IRB meeting.
Jul 30, 2026 @ 1:00 PM
My Study Was Approved…Now What? Ongoing Submissions“Ongoing Submissions” will focus on post-approval IRB submissions including amendments (modifications), continuing reviews, deviations, reportable events, exception requests, annual check-ins, and closures. Presenters will define each submission type, discuss when they are needed, and review what they should include. This session will focus on the substance of each submission type with brief overviews of how to technically submit them in eIRB. The session will be relevant to investigators at all levels who conduct non-exempt research. You must register to attend. Please contact Diana Floegel with any questions or if you have trouble registering!
Aug 3, 2026 @ 11:30 AM
IRB 1Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 5, 2026 @ 11:00 AM
IRB 7Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 7, 2026 @ 10:00 AM
IRB 3Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 10, 2026 @ 12:00 PM
IRB 8Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 13, 2026 @ 1:00 PM
Informed Consent 101“Informed Consent 101” will review expectations for obtaining consent from participants in biomedical and social-behavioral research. Content will include required elements of consent, HIPAA authorization, tips for making consent a process rather than an event, and criteria that need to be met for alterations and waivers of consent to be approved. This session is relevant for both biomedical and social-behavioral researchers including faculty, staff, and students. You must register to attend. Please contact Diana Floegel with any questions or if you have trouble registering!
Aug 18, 2026 @ 10:45 AM
IRB 4Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 20, 2026 @ 11:45 AM
IRB 2Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Aug 25, 2026 @ 12:00 PM
IRB 10Video Conferencing/Lancaster General Hospital 555 North Duke St Lancaster, PA 17602
Aug 26, 2026 @ 12:00 PM
IRB 5Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Sep 2, 2026 @ 11:00 AM
IRB 7Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
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